Canonical Allele Identifier: CA2617153427
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273659_4273688del , CM000674.2:g.4273659_4273688del GRCh38
NC_000012.11:g.4382825_4382854del , CM000674.1:g.4382825_4382854del GRCh37
NC_000012.10:g.4253086_4253115del NCBI36
NG_034254.1:g.4924_4953del

Transcript Alleles

HGVS Amino-acid Change
ENST00000676279.1:c.-40-342_-40-313del (CCND2) ENSP00000502597.1:n.-40-342_-40-313del
ENST00000676411.1:c.-40-342_-40-313del (CCND2) ENSP00000502654.1:n.-40-342_-40-313del
NR_125790.1:n.126+2372_126+2401del (CCND2-AS1)
NR_149145.1:n.182+1609_182+1638del (CCND2-AS1)
NR_149146.1:n.182+1609_182+1638del (CCND2-AS1)